Building a zoo of mice for genetic analyses: A comprehensive protocol for the rapid generation of BAC transgenic mice

Transgenic mice are highly valuable tools for biological research as they allow cell type–specific expression of functionally instrumental genes. In this protocol, the generation of bacterial artificial chromosome (BAC) transgenic constructs is described. We give an overview of different transgenic...

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Published in:Genesis (New York, N.Y. : 2000) Vol. 48; no. 4; pp. 264 - 280
Main Authors: Johansson, Torbjörn, Broll, Ilja, Frenz, Theresa, Hemmers, Saskia, Becher, Burkhard, Zeilhofer, Hanns Ulrich, Buch, Thorsten
Format: Journal Article
Language:English
Published: Hoboken Wiley Subscription Services, Inc., A Wiley Company 01-04-2010
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Summary:Transgenic mice are highly valuable tools for biological research as they allow cell type–specific expression of functionally instrumental genes. In this protocol, the generation of bacterial artificial chromosome (BAC) transgenic constructs is described. We give an overview of different transgenic inserts, such as fluorescent proteins (alone or in combination with Cre variants), diphtheria toxin receptor, lacZ, and light‐activated ion channels. The most reliable and versatile approach to express these genes is by using BACs, which allow “highjacking” of the expression pattern of a gene without characterizing its transcriptional control elements. Here, we describe the necessary cloning techniques compared with conventional transgenesis. With the provided “toolbox” of already available transgene constructs, the generation of the BAC transgenes is made easy and rapid. We provide a comprehensive outline how to insert the different transgenes into a chosen BAC by either ET cloning or recombineering. We also describe in detail the methods to identify the correct insertion and the integrity of the final BAC construct, and finally, the preparation of the BAC DNA for oocyte injection is described. genesis 48:264–280, 2010. © 2010 Wiley‐Liss, Inc.
Bibliography:ArticleID:DVG20612
NCCR-Neuro (CTE)
istex:9D94FA6724DFCCD2EF0849D632B0F59493C90576
Deutsche Forschungsgemeinschaft - No. BU 1410/1-2
ark:/67375/WNG-1CXQHWKZ-M
Swiss National Science Foundation - No. 310000-116201/1; No. CRSI33_125073; No. 3100A0-116064/1; No. 3100A0-116070/1
Torbjörn Johansson and Ilja Broll contributed equally to this work.
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ISSN:1526-954X
1526-968X
DOI:10.1002/dvg.20612